Canonical Allele Identifier: PA2826128852
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 944744
ClinVar RCV Id: RCV001841186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171273.1:p.Ile48Thr
CA397994212
NM_001177802.2:c.143T>C